Residual Risk and Risk based Verification - Webinar By GlobalCompliancePanel

Learn how define the residual risk of your device and how to streamline the verification process by employing a risk based approach. 

Adjusting the verification process to account for the criticality of the verified items can drastically reduce the overall cost and time for verification activities. By implementing a risk based verification approach activities at the end of the device development can be streamlines and the time to market can be shortened without compromising the safety or effectiveness of the medical device.

Areas Covered in the Session

Residual risk identification and declaration    Risk based verification techniques    Objective base verification planning    Documentation of verification activities    Practical tips for verifying system and software requirements  

Who Will Benefit:

Project Managers System Engineers Test and Verification Engineers Regulatory Affairs Compliance Managers Regulatory and Compliance Associates

 

Price List: Live : $245.00 Corporate live : $995.00 Recorded : $295.00   webinars@globalcompliancepanel.com http://www.globalcompliancepanel.com   Phone: 800-447-9407 Fax: 302-288-6884   Tuesday, August 9, 2011  
10:00 AM PDT | 01:00 PM EDT